Central clot stabilizer and manipulator

ABSTRACT

A clot encasement and removal device for removing a vascular obstruction is disclosed. The encasement device comprises proximal and distal capture members and a central stabilizer. The central stabilizer provides several points of contact for interacting with and manipulating an intravascular obstruction. The central stabilizer may be coupled to the distal capture member, allowing the central stabilizer and distal capture member to be manipulated in unison. The central stabilizer may reside on a distinct delivery wire, enabling independent control of proximal and distal capture members and the central stabilizer. The proximal capture member may comprise a furrowed delivery wire to enable retraction of at least a portion of the central stabilizer within the proximal capture member.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. Non-Provisional patentapplication Ser. No. 16/319,231 filed on Jan. 18, 2019, which is anational phase application under 35 U.S.C. § 371 that claims priority toInternational Application No. PCT/US2017/043282 filed Jul. 21, 2017,which claims priority to U.S. Provisional Application No. 62/365,472filed Jul. 22, 2016, all of which are incorporated herein by referencein their entirety.

TECHNICAL FIELD

Embodiments of the present disclosure relate generally to medicaldevices and methods of using same, and more specifically, to medicaldevices for treating, including treating an occluded biological lumen,such as an embolus or clot in a blood vessel.

BACKGROUND

This section is intended to introduce various aspects of the art, whichmay be associated with exemplary embodiments of the present disclosure.This discussion is believed to assist in providing a framework tofacilitate a better understanding of particular aspects of the presentdisclosure. Accordingly, it should be understood that this sectionshould be read in this light, and not necessarily as any admission ofprior art.

There are many reasons a blood vessel becomes blocked or obstructed. Oneway is from deposition of thrombus on the walls of the blood vessels.The buildup of these clots can restrict blood flow. Because arterialblockages reduce blood flow through the affected vessel, any blockage orobstruction can lead to many serious medical complications. Forinstance, tissue relying on the blood's supply of oxygen may becomedamaged due to the decrease in the oxygen amount or the blockage canresult in a heart attack if the obstructed vessel supplies blood to theheart itself.

While various methods are available to treat a blockage or obstructionthrough removal of the obstruction, these methods do not sufficientlycapture and retain the particulate matters from the obstruction toprevent them from migrating to another area of the vascular system wherethey can get lodged again.

The present disclosure provides solutions to long-felt needs in the artto treat occluded vessels.

SUMMARY

The foregoing has outlined rather broadly the features and technicaladvantages of the embodiments of the present disclosure in order thatthe detailed description of these embodiments that follows may be betterunderstood. Additional features and advantages of the embodiments of thepresent disclosure will be described hereinafter which form the subjectof the claims of the present disclosure. It should be appreciated bythose skilled in the art that the conception and specific embodimentdisclosed may be readily utilized as a basis for modifying or designingother structures for carrying out the same purposes of the presentdisclosure. It should also be realized by those skilled in the art thatsuch equivalent constructions do not depart from the spirit and scope ofthe present disclosure as set forth in the appended claims. The novelfeatures which are believed to be characteristic of the presentdisclosure, both as to its organization and method of operation,together with further objects and advantages will be better understoodfrom the following description when considered in connection with theaccompanying figures. It is to be expressly understood, however, thateach of the figures is provided for the purpose of illustration anddescription only and is not intended as a definition of the limits ofthe present disclosure.

The term “coupled” is defined as connected, although not necessarilydirectly, and not necessarily mechanically. The terms “a” and “an” aredefined as one or more unless this disclosure explicitly requiresotherwise. The term “substantially” is defined as being largely but notnecessarily wholly what is specified (and include wholly what isspecified) as understood by one of ordinary skill in the art. In anydisclosed embodiment, the term “substantially” may be substituted with“within [a percentage] of” what is specified, where the percentageincludes 0.1, 1, 5, and 10 percent. The terms “comprise” (and any formof comprise, such as “comprises” and “comprising”), “have” (and any formof have, such as “has” and “having”), “include” (and any form ofinclude, such as “includes” and “including”) and “contain” (and any formof contain, such as “contains” and “containing”) are open-ended linkingverbs. As a result, an encasement sleeve that “comprises,” “has,”“includes” or “contains” one or more elements possesses those one ormore elements, but is not limited to possessing only those one or moreelements Likewise, an element of a system or composition that“comprises,” “has,” “includes” or “contains” one or more featurespossesses those one or more features, but is not limited to possessingonly those one or more features. Furthermore, a structure or compositionthat is configured in a certain way is configured in at least that way,but may also be configured in ways that are not listed. Metric units maybe derived from the English units provided by applying a conversion androunding to the nearest millimeter. The feature or features of oneembodiment may be applied to other embodiments, even though notdescribed or illustrated, unless expressly prohibited by this disclosureor the nature of the embodiments. Any embodiment of any of the disclosedcontainer assemblies and compositions can consist of or consistessentially of—rather than comprise/include/contain/have—any of thedescribed elements and/or features and/or steps. Thus, in any of theclaims, the term “consisting of” or “consisting essentially of” can besubstituted for any of the open-ended linking verbs recited above, inorder to change the scope of a given claim from what it would otherwisebe using the open-ended linking verb. Details associated with theembodiments described above and others are presented below.

Embodiments of the disclosure are directed towards a clot encasement andremoval device. In particular embodiments, the device comprises proximaland distal capture members within which a clot or other obstruction maybe sequestered. In specific aspects, the device further comprises acentral stabilizer for direct contact, stabilization, and manipulationof a vascular obstruction. The central stabilizer may be used at leastin part to effectively grab an obstruction. The central stabilizer maybe operated in unison with the proximal capture member, or it may beindependently operated. In some embodiments, the proximal capture memberfeatures a furrowed section for allowing at least a portion of thecentral stabilizer to be withdrawn into the proximal capture member.

The clot encasement device is configured to offer a multitude of optionsfor capturing and manipulating obstructions. Upon making contact andstabilizing an obstruction, the central stabilizer may be pulled intothe proximal capture member, the stabilizer may be pushed into thedistal capture member, or either or both of the capture members may bedirected to encase at least a portion of the central stabilizer. Thecentral stabilizer may hold an obstruction in place, and the proximaland/or distal capture members may be manipulated to encase theobstruction. Both proximal and distal capture members may come togetherto provide an encasing volume for the obstruction. The proximal anddistal capture members may comprise frame components at open ends withthe same or different diameters. The diameters may be selected such thatone frame fits within the other frame, at least in part. In thisfashion, the proximal and distal capture members can provide a tightseal around an obstruction, thereby preventing obstruction outflow orescape.

In some embodiments, a device for removal of an obstruction in a lumencomprises a proximal capture member and a distal capture member. Inspecific embodiments, the proximal capture member comprises a proximalencasement sleeve and a hollow proximal delivery wire, and the distalcapture member comprises a distal encasement sleeve and a discontinuousdelivery wire. In some embodiments, the a central stabilizer is includedand bisects the discontinuous delivery wire into proximal and distalsegments.

The shape of the central stabilizer is different from the shape of thedelivery wire to which it is coupled. In some embodiments, across-sectional shape of at least a portion of the central stabilizer isdifferent from a cross-sectional shape of the distal segment of thediscontinuous delivery wire. In some aspects, at least a portion of theproximal segment of the discontinuous delivery wire lies within thehollow proximal delivery wire.

In some embodiments, each of the proximal and distal capture membersfurther comprises an open end and a tapered end, and a frame componentcoupled to a encasement sleeve. The encasement sleeve extends betweenthe open end and tapered end. The proximal frame component, distal framecomponent, and/or central stabilizer may comprise a self-expandingmaterial. In some embodiments, the proximal frame component, distalframe component, and/or central stabilizer have a collapsedconfiguration and an expanded configuration. The device may furthercomprises a catheter, within which the proximal frame component, distalframe component, and central stabilizer reside in the respectivecollapsed configurations.

In some aspects, at least one of the distal or proximal capture memberscomprises a support arm. The support arm may be coupled to therespective delivery wire and the respective frame component. Theproximal or distal capture members may further comprise a fasteningcomponent slidably coupled to the respective delivery wire, therebyallowing a coupling angle of the respective frame component to beadjusted.

In some aspects, the encasement sleeves comprise a woven material of atleast one of the following: a polymer, a metal, and any combinationthereof. In some embodiments, the encasement sleeves are devoid of anyfenestrations. The encasement sleeves may be made of a soft and flexiblematerial. In some aspects, the encasement sleeves comprise aself-expanding material configured to bias the encasement sleeve into anexpanded configuration. In some aspects, each encasement sleeve isconfigured to cover at least a portion of a surface of the framecomponent to which it is coupled. In some aspects, at least one of theproximal frame component, the distal frame component, or the centralstabilizer may be configured to deliver a therapeutic substance to saidobstruction.

The clot encasement device may comprise at least one radiopaque marker.In some aspects, each delivery wire comprises at least one radiopaquemarker. In further aspects, each delivery wire comprises at least tworadiopaque markers.

The clot encasement device may be configured to allow the centralstabilizer to be withdrawn into the proximal capture member. In someaspects, at least a portion of the proximal hollow delivery wirecomprises a furrowed semi-cylinder that allows at least a portion thecentral stabilizer to be withdrawn into the proximal encasement sleeve.In some embodiments, the furrowed semi-cylinder comprises a length thatis equal to or greater than a central stabilizer length to allow theentire length of the central stabilizer to reside within the proximalencasement sleeve. In some embodiments, a proximal frame componentdiameter is different from a distal frame component diameter, therebyallowing one frame component to fit within the other frame component.

Some aspects of the disclosure are directed towards a clot encasementdevice comprising, a proximal capture member coupled to a proximaldelivery wire, a distal capture member coupled to a distal deliverywire, and a central stabilizer coupled to a central delivery wire thatis distinct from the distal delivery wire, thereby allowing independentmanipulation of the proximal and distal capture members and the centralstabilizer. In some aspects, each of the proximal and distal capturemembers further comprises an open end and a tapered end, a framecomponent coupled to a encasement sleeve, with the encasement sleeveextending between the open and tapered ends. In some embodiments, theproximal frame component, distal frame component, and/or centralstabilizer comprise a self-expanding material configured to have acollapsed configuration and an expanded configuration. The devicecomprises a catheter, within which the proximal frame component, distalframe component, and central stabilizer reside in their respectivecollapsed configurations.

In some embodiments, at least a portion of the central stabilizercomprises a cross-sectional shape that is different from across-sectional shape of the central delivery wire. In some embodiments,the central delivery wire and the distal delivery wire lie adjacent toeach other within the hollow proximal delivery wire. In otherembodiments, the central delivery wire and distal delivery wire areoriented concentrically within the hollow proximal tube. In someembodiments, at least a portion of the central delivery wire resideswithin at least a portion of the distal delivery wire. In some aspects,at least a portion of the hollow proximal delivery wire or the distaldelivery wire comprises a furrowed semi-cylinder that allows at least aportion the central stabilizer to be maneuvered into the respectiveencasement sleeve. In some embodiments, the furrowed semi-cylinderlength is equal to or greater than the length of central stabilizer,enabling the entire length of the central stabilizer to be maneuveredinto the proximal or distal encasement sleeve.

In some embodiments of the clot encasement device, at least one capturemember is coupled to a support arm. The support arm may be coupled tothe respective delivery wire and the respective frame component. Atleast one capture member may further comprise a fastening componentslidably coupled to the respective delivery wire, thereby allowing acoupling angle of the respective frame component to be adjusted.

In some aspects, the encasement sleeves comprise a woven material of atleast one of the following: a polymer, a metal, and any combinationthereof. In some embodiments, the encasement sleeves are devoid of anyfenestrations. The encasement sleeves may be made of a soft and flexiblematerial. In some aspects, the encasement sleeves comprise aself-expanding material configured to bias the encasement sleeve into anexpanded configuration. In some aspects, each encasement sleeve isconfigured to cover at least a portion of a surface of the framecomponent to which it is coupled. In some aspects, at least one of theproximal frame component, the distal frame component, or the centralstabilizer may be configured to deliver a therapeutic substance to saidobstruction.

The clot encasement device may comprise at least one radiopaque marker.In some aspects, each delivery wire comprises at least one radiopaquemarker. In further aspects, each delivery wire comprises at least tworadiopaque markers.

BRIEF DESCRIPTION OF THE DRAWINGS

The following drawings illustrate by way of example and not limitation.For the sake of brevity and clarity, every feature of a given structuremay not be labeled in every figure in which that structure appears.

FIG. 1 is a side perspective view of a first embodiment of the clotencasement and removal system. The central clot stabilizer is in theform of a brush and is coupled to the distal capture member.

FIG. 2 is a side perspective view of a second embodiment of the clotencasement and removal system. The central clot stabilizer is in theform of a coil and is coupled to the distal capture member.

FIG. 3 is a side perspective view of a third embodiment of the clotencasement and removal system. The central clot stabilizer is in theform of a lemniscate and is coupled to the distal capture member.

FIG. 4 is a side perspective view of a fourth embodiment of the clotencasement and removal system. The central clot stabilizer is in theform of a brush. The central clot stabilizer and distal capture memberare coupled to distinct delivery wires.

FIG. 5 is a perspective view of a hollow proximal delivery wire with afurrowed semi-cylinder. The furrow allows at least a portion the centralstabilizer to be withdrawn into the proximal encasement sleeve.

FIGS. 6A-6C depict three views of a proximal hollow delivery wire with afurrowed semi-cylinder. FIG. 6A is a top view of the distal deliverywire residing within the hollow proximal delivery wire. FIG. 6B is across-sectional view of the distal delivery wire residing within anon-furrowed section of the hollow proximal delivery wire. FIG. 6C is across-sectional view of the distal delivery wire residing within afurrowed section of the hollow proximal delivery wire.

FIGS. 7A-7B depict one embodiment of the clot encasement and removalsystem wherein the central clot stabilizer is manually adjustable. FIG.7A depicts the manually adjustable central clot stabilizer in apartially-collapsed state. FIG. 7B depicts the manually adjustablecentral clot stabilizer in an expanded state.

DETAILED DESCRIPTION

Embodiments of the present disclosure provide for minimally invasiveremoval of accumulated material, such as a clot or embolism, disposed ina patient's (mammalian, including human or otherwise) vascular system.Certain embodiments of the present disclosure are particularlyapplicable for extraction of material in distal, narrow, tortuoussegments of the neuro-blood vessels. In a general embodiment, theendovascular device of the present disclosure includes two opposingcapture members that are slidably coupled to each other. Each capturemember preferably comprises an open end and a tapered end, where theopen end of each capture member face one another. In one embodiment, theendovascular device can be delivered to the site of the material depositusing a catheter. The capture members can be placed on each side of thematerial deposit with the open ends facing the material deposit.Preferably, the majority of the material deposit is moved into thecapture members when the capture members progresses toward one another.In one closed configuration, the open end of the capture members meetone another to form an enclosure to capture and retain the materialdeposit contained therein. The capture members can be withdrawn in thisclosed configuration and/or be pulled into a catheter, thereby removingthe material deposit.

FIGS. 1-6 show certain specific embodiments according to the aspects ofthe present invention. FIGS. 1-3 depict a side perspective view of threeembodiments of the clot encasement and removal system. The threeembodiments differ in the shape of the central clot stabilizer. Theembodiment depicted in FIG. 1 includes a brush-like central clotstabilizer. The embodiment depicted in FIG. 2 includes a coil-shapecentral clot stabilizer. The embodiment depicted in FIG. 3 includes alemniscate-shaped central clot stabilizer.

As shown in FIG. 1, the clot encasement and removal system comprises twocapture members 110 and 112. Capture member 112 is the distal capturemember and capture member 110 is the proximal member. The proximal anddistal qualifiers describe the relative distances from a care provider(e.g., physician) who may be using the clot encasement device.

Proximal capture member 110 comprises a proximal encasement sleeve 114and a hollow proximal delivery wire 116. Distal capture member 112comprises a distal encasement sleeve 118 and a discontinuous deliverywire 120. The discontinuous delivery wire 120 is divided into distalsegment 120 a and proximal segment 120 b. Distal and proximal segmentsof the discontinuous delivery wire 120 are bisected by a centralstabilizer 122. Bisection of the discontinuous delivery wire 120 by thecentral stabilizer 122 does not necessarily divide distal and proximalsegments of the discontinuous delivery wire 120 into two equal parts,such that the distal and proximal segments 120 a and 120 b may ofdifferent lengths.

At least a portion of the central stabilizer 122 comprises across-sectional shape that is different from the cross-sectional shapeof the distal segment 120 a of the discontinuous delivery wire 120. Insome embodiments, the cross-sectional shape of the distal segment of thediscontinuous delivery wire is circular. The cross-sectional shape ofcentral stabilizer 122 may be constant or may vary along the length ofthe central stabilizer 122. The cross-sectional shape at least one pointalong the length of the central 122 is different from thecross-sectional shape of the distal segment 120 a of the discontinuousdelivery wire 120.

At least a portion of the proximal segment 120 a of the discontinuousdelivery wire 120 resides within the hollow proximal delivery wire 116.The inclusion of two distinct delivery wires, hollow proximal deliverywire 116 and the discontinuous delivery wire 120, allows the proximaland distal capture members to be maneuvered independently. The proximalcapture member 110 and the distal capture member 112 may also bemaneuvered in unison.

As depicted in FIG. 5, the hollow proximal delivery wire 516 maycomprise a furrowed semi-cylinder. The furrow allows at least a portionof the central stabilizer to be withdrawn into the proximal encasementsleeve. The length of the furrow may be selected based upon theparticular application. In some embodiments, the furrow may be of alength that allows a portion of the central stabilizer to be withdrawninto the proximal encasement sleeve. In other embodiments, the furrowmay be of a length that allows the entire length of the centralstabilizer to be withdrawn into the proximal encasement sleeve. Thefurrow provides the hollow proximal delivery wire with an open sectionthrough which the central stabilizer may pass. In this fashion, the openfurrowed area prevents the central stabilizer from collapsing to fitwithin the proximal delivery wire hollow.

The hollow proximal delivery wire 116 and discontinuous delivery wire120 may comprise a radiopaque material. Non-limiting examples of aradiopaque material include platinum or tantalum DFT Nitinol. Theradiopaque material provides a radiopaque marker that may be used to aimand maneuver different sections of the clot encasement. The embodimentdepicted in FIG. 1 includes four distinct radiopaque markers which arelocated on the hollow proximal delivery wire 116 and discontinuousdelivery wire 120. The discontinuous delivery wire 120 comprisesradiopaque markers 134 a and 134 b. The hollow proximal delivery wire116 comprises radiopaque markers 134 c and 134 d. In this embodiment,the radiopaque markers are located at open and tapered sections ofproximal encasement sleeve 114 and distal encasement sleeves 118. Thelocation and number of radiopaque markers is not limited to the locationand number of radiopaque markers depicted in FIG. 1. Radiopaque markersmay be located at any location on the clot encasement device. Any numberof radiopaque markers may be incorporated into the clot encasementdevice. For example, a clot encasement device may include 0, 1, 2, 3, 4,5, 6, or more radiopaque markers.

Proximal capture member 110 and distal capture member 112 may furthercomprise a frame component. The frame component may be coupled to anopen end of the encasement sleeve. The frame component may be coupled tothe capture member delivery wire. The frame component aids in providingrigidity for maintaining the shape and size of open ends of encasementsleeves in expanded configurations. Frame components are preferablycircular in shape to match the shape of the target blood vessel. Inother embodiments, however, frame components can have any shape in theexpanded configuration desired, such as circular, oval, rectangular orany other regular or irregular shapes that may be suitable to theparticular application. In the embodiment depicted in FIG. 1, distalframe component 128 is coupled to the open end of distal encasementsleeve 118 and to hollow proximal delivery wire 116. Proximal framecomponent 126 is coupled to the open end of proximal encasement sleeve114 and to the distal segment 120 a of discontinuous delivery wire 120.

The angle between a frame component and a delivery wire may be fixed ormay be adjustable. Proximal capture member 110 and/or distal capturemember 112 may further comprise a fastening component slidably coupledto the respective delivery wire. The fastening component allows acoupling angle of the respective frame component to be adjusted. In theembodiment depicted in FIG. 1., proximal capture member 110 comprisesproximal fastening component 130, which is coupled to hollow proximaldelivery wire 116 and proximal frame component 126. Distal capturemember 112 comprises distal fastening component 132, which is coupled tothe distal segment 120 a of distal delivery wire 120 and distal framecomponent 128.

The size and shape of the proximal and distal frame components may bethe same or different. In one embodiment, the proximal frame component126 and distal frame component 128 are both circular in shape. Thediameter of proximal frame component 126 is different from the diameterof distal frame component 128. The diameters (or other size for anon-circular frame) of the proximal and distal frame components may beselected such that one frame component fits within the other framecomponent. This allows the frame components, and the encasement sleevesto which they are coupled, to fit within one another, thereby providingan encasement volume within which an obstruction may be captured. Thesized of the proximal and distal frame components may be selected toprovide a tight junction between open ends of respective capturemembers.

Frame components preferably comprises a superelastic and/orself-expanding material. In particular, the superelastic and/orself-expanding material preferably have properties that allow it to havea deformed shape under one condition and to recover its original shapeprior to deformation, which can also be referred to as an expandedconfiguration, in response to exposure to an activation mechanism.Preferably, the material can include a memory-shaped heated alloy suchas nitinol, or nickel titanium, which is a metal alloy of nickel andtitanium. Nitinol alloys exhibit two closely related and uniqueproperties: shape memory and superelasticity. Shape memory refers to theability of nitinol to undergo deformation at one temperature, thenrecover its original, un-deformed shape upon heating above its“transformation temperature.” That is, nitinol alloy has a biasedexpanded condition and may be compressed into a collapsed or deformedcondition before use. During use, it may be exposed to temperature abovethe transformation threshold, thereby causing it to revert back to itsun-deformed and/or original shape. Frame components can also compriseany flexible and/or elastic material that allows frame components to becompressed, or deformed by a radial force, to fit into a catheter, suchas catheter 124 shown in FIG. 1, without sustaining any damage andrevert back to its original shape once released from the catheter.

In one embodiment, the diameter of frame components 126 and 128 rangesbetween about 10 microns to 500 microns. In a preferred embodiment, thediameter of frame components 126 and 128 ranges between about 80 micronsto about 120 microns. In another preferred embodiment, the diameter offrame components 126 and 128 ranges between about 95 microns to about105 microns.

The diameter of at least one of frame components 126 and 128 in theexpanded configuration, and capture member open ends, is preferablyconfigured to substantially match the diameter of the particular lumenor blood vessel of interest in which the target material deposit, e.g.,clot, is disposed. In such an expanded configuration, frame components126 and/or 128 preferably contact the inner wall of the target bloodvessel gently, e.g., without exerting significant force that can damagethe blood vessel. This allows at least one capture member 110 or 112 toextend across the interior, or lumen, of the blood vessel whereeffectively most or all the fluid and material flowing through thetarget blood vessel are directed through the respective extended capturemember 110 or 112. In one embodiment, the diameter of at least oneencasement sleeve open end is in a range of about 1.5 mm to about 6 mm,and preferably in a range of about 2 mm to about 4.5 mm. In anotherpreferred embodiment, the diameter of at least one encasement sleeveopen end is between about 2.5 mm and about 3 mm.

The clot encasement device comprises a central stabilizer. In someembodiments, the central stabilizer comprises a self-expanding materialconfigured to have a collapsed configuration and an expandedconfiguration. The central stabilizer functions to provide one or morepoints of contact with an obstruction, e.g., a clot. Contacting anobstruction with the central stabilizer allows the central stabilizer toexert a stabilizing force on the obstruction. Obstruction stabilizationis especially useful for long clots (>5 mm). The centralstabilizer/obstruction contact may occur at either end of theobstruction, between ends of the obstruction, or along the entire lengthof the obstruction. Contacting an obstruction with the centralstabilizer allows the obstruction to be stabilized, or held in place.The obstruction may be stabilized by the central stabilizer while movingone or both capture members over the obstruction surface to encapsulatethe obstruction without significant compression and/or deformation.Contacting an obstruction with the central stabilizer may be used toapply a dragging force uniformly at one or more points along the lengthof the obstruction. In this fashion, the central stabilizer may be usedto effectively manipulate the obstruction at least partially inside oneor both capture members. Manipulation of an obstruction may beaccomplished without significant compression and deformation of theclot.

In further embodiments, the central stabilizer is manually adjustable.Manual adjustment of the central stabilizer allows the user to controlthe central stabilizer expansion state. The central stabilizer mayreside within the hollow proximal delivery wire in a fully or partiallycollapsed state. Upon being directed or manipulated out of the hollowproximal delivery wire, the central stabilizer may remain in a fullycollapsed state. The central stabilizer may include one or moreradiopaque markers to assist in delivery and placement of the centralstabilizer relative to an obstruction. The expansion state of thecentral stabilizer may be manually adjusted from fully collapsed tofully expanded, or any expansion state therebetween. FIG. 7A depicts themanually adjustable central clot stabilizer in a partially-collapsed orpartially-expanded state. FIG. 7B depicts the manually adjustablecentral clot stabilizer in an expanded state. The expansion state of thecentral clot stabilizer may be selected and adjusted to optimallyposition, grasp, prod, penetrate, pierce, nudge, envelop, clasp, and/orretrieve an obstruction.

The central stabilizer 122 may be at least partially withdrawn into theproximal encasement sleeve. The hollow proximal delivery wire maycomprise a furrow whose shape and size are selected to allow at least aportion of the central stabilizer to overlap at least a portion of thelength of the hollow proximal delivery wire 116. In this fashion, thecentral stabilizer may be withdrawn into the proximal encasement sleeve.The central stabilizer 122 may be provided with or have incorporatedwithin it a radiopaque material. The central stabilizer 122 may compriseone or more radiopaque markers.

The size and shape of the central stabilizer may be selected dependingon the blood vessel and obstruction. The central stabilizer size may beselected such that a portion of, or the entirety of the centralstabilizer fits within at least one encasement sleeve. The orthogonalsize of the central stabilizer may range from about 1 to about 6 mm, andpreferably from about 2 mm to about 3 mm. The orthogonal size refers tothe dimension of the central stabilizer that is orthogonal to the linecreated by the delivery wires. The length of the central stabilizer mayrange between about 5 mm to about 40 mm, and preferably from about 10 mmto about 20 mm. The central stabilizer may comprise a superelasticand/or self-expanding material. In particular, the superelastic and/orself-expanding material preferably have properties that allow it to havea deformed shape under one condition and to recover its original shapeprior to deformation, which can also be referred to as an expandedconfiguration, in response to exposure to an activation mechanism. Thecentral stabilizer material can include a memory-shaped metal or alloysuch as nitinol, or nickel titanium, which is a metal alloy of nickeland titanium. In some embodiments, the central stabilizer may be made ofa polymer. In further embodiments, the central stabilizer is made of acombination of a polymer and a memory-shaped metal or alloy.

The central stabilizer is provided in a shape that is different from thedelivery wire shape. In some embodiments, the cross-sectional shape ofat least a portion of the central stabilizer is different from across-sectional shape of the distal segment of the discontinuousdelivery wire. A discontinuous delivery wire cross-sectional shape maybe square, round, oval, rectangular, etc. The central stabilizer isshaped such that at least a portion of the central stabilizer'scross-sectional shape is different from the discontinuous delivery wirecross-sectional shape. In comparison to the delivery wire, the centralstabilizer shape provides a different or additional surface area forengaging an obstruction. The central stabilizer shape may be a helix, adouble helix, a lemniscate, a coil or spring, or a brush withprojections emanating from a base. A helix, double helix, or coil orspring may have ring coils with the same or different diameters. Thering coil diameters may be constant along the central stabilizer lengthor they may be variable. The ring coil diameters may increase or taperin size. The ring coil diameters may be of alternating diameters. Thehelix, spring, or coil may be wound clockwise or counterclockwise. Thecoil pitch may be tight, for example, 0.5 mm. The coil pitch may beintermediate, for example 1 mm to 2 mm. The coil pitch may be loose, forexample 3 mm and above. The coil pitch may vary from about 0.5 mm toabout 5 mm. The coil rings may be touching or they may be separated. Adouble helix may comprise two component helices with the same ordifferent dimensions. In some embodiments, a central stabilizercomprises a plurality of component wires. In some embodiments, a centralstabilizer comprises a braided shape, for example, a bi-axial orhigher-order braid. In central stabilizer embodiments comprising aplurality of component wires, the wires may be separate from each otheror may be attached to each other at one or more points. In abrush-shaped central stabilizer, the projections may be of uniformlength or of varying length. The distance between the projections may beconstant or may vary. In some embodiments, the distance betweenprojections varies from about 0.5 mm to about 3 mm. The projection anglemay vary from acute to obtuse. In a preferred embodiment, the projectionangle is 90 degrees. In some embodiments, a central stabilizer maycomprise a combination of different shapes.

The distal and proximal encasement sleeves may be formed of any materialwhich is flexible and compatible with bodily fluids such as blood.Non-limiting examples of suitable materials include polymeric filmmaterials, such as, but not limited to, polyurethane, polyolefin,polyester, and silicone polymers. In an embodiment using such polymericfilm material, distal and/or proximal encasement sleeve tapered ends canfurther include apertures of sufficient size to allow fluids to flowthrough distal and/or proximal encasement sleeve while retaining thecaptured material deposit. In some embodiments, distal and/or proximalencasement sleeves comprise a polymeric net-like material having aplurality of apertures throughout the material, such as, but not limitedto, a woven mesh of polymeric material, metal, and/or othersuperelastic, self-expanding, and/or memory shape alloy such as nitinol.In certain embodiments, the woven mesh can comprise a combination ofpolymers, metals, and/or metal alloys. While the figures may depict bodymembers formed of a film material, it is intended to be exemplary andnot limiting, as it is understood that such body members can be made ofnet-like material without departing from certain aspects of the presentinvention. In one embodiment, the material of distal and/or proximalencasement sleeve can comprise material similar to that of the materialof frame component, providing it a biased shape in the expandedconfiguration that allows distal and/or proximal encasement sleeve toremain open as it extends away from its respective frame component. Insome embodiments, the total length of distal and proximal encasementsleeves is between about 5 mm and about 30 mm. In a preferredembodiment, the total length of both distal and proximal encasementsleeves is between about 8 mm and about 20. In another preferredembodiment, the total length of distal and proximal encasement sleevesis between about 10 mm and 12 mm. In yet another preferred embodiment,the total length of distal and proximal encasement sleeves is about 10mm.

In one embodiment, a user can hold hollow proximal delivery wire 116static, thereby keeping proximal capture member 110 in one position,while pushing or pulling distal guide member 120 to adjust the positionof distal capture member 112. In another embodiment, the user can holddistal guide member 120 constant, thereby keeping distal capture member112 in one position, while pushing or pulling hollow proximal deliverywire 116 to adjust the position of proximal capture member 110. In yetanother embodiment, both delivery wires 116 and 120 can be adjusted atthe same time to achieve the desired positions of capture members 110and 112 and central stabilizer 122.

The body of either delivery wire 116 or 118 preferably has a lengthsufficient to extend through the vascular system of a patient to reachthe target accumulation and place endovascular device in the desireddeployment location. In one embodiment, either delivery wire 116 or 118has a length of between about 50 cm and about 250 cm, more preferably alength of about 125 cm and about 175 cm. The diameter of either deliverywire 116 or 118 may be constant or may vary along the length of therespective delivery wire 116 or 118. For example, the diameter of oneguide member toward the proximal end away from the user may be betweenabout 0.2 mm and about 1 mm, and preferably about 0.3 mm and about 0.4mm, while the diameter near the distal end near the clot may be betweenabout 0.05 mm and about 1 mm, and more preferably about 0.1 mm and about0.2 mm. Accordingly, the diameter of either guide member 116, 118 maytaper from the proximal end to the distal end.

Referring to FIG. 4, some embodiments of a clot encasement device maycomprise a proximal capture member coupled to a hollow proximal deliverywire, a central stabilizer coupled to a central delivery wire and adistal capture member coupled to a distal delivery wire. The central anddistal delivery wires are distinct wires which allow independent controlof the respective central stabilizer and distal capture member. At leasta portion of the central and distal delivery wires reside within thehollow proximal delivery wire, and are controlled by manipulationthrough the interior of the hollow proximal delivery wire. Each of theproximal, central, and distal delivery wires may comprise at least oneradiopaque marker. The radiopaque marker enables visualization of therespective delivery wire to which the marker is coupled. The proximal,central, and distal delivery wires may be independently controlled forindependent manipulation of the respective proximal capture member,central stabilizer, and distal capture member.

Although the embodiments of the present disclosure and their advantageshave been described in detail, it should be understood that variouschanges, substitutions and alterations can be made herein withoutdeparting from the spirit and scope of the invention as defined by theappended claims. Moreover, the scope of the present application is notintended to be limited to the particular embodiments of the process,machine, manufacture, composition of matter, means, methods and stepsdescribed in the specification. As one of ordinary skill in the art willreadily appreciate from the present disclosure, processes, machines,manufacture, compositions of matter, means, methods, or steps, presentlyexisting or later to be developed that perform substantially the samefunction or achieve substantially the same result as the correspondingembodiments described herein may be utilized according to the presentdisclosure. Accordingly, the appended claims are intended to includewithin their scope such processes, machines, manufacture, compositionsof matter, means, methods, or steps.

1. A device for remove an obstruction in a lumen comprising: a proximalcapture member; and a distal capture member; wherein the proximalcapture member comprises a proximal encasement sleeve and a hollowproximal delivery wire; wherein the distal capture member comprises adistal encasement sleeve and a discontinuous delivery wire; a centralstabilizer bisecting the discontinuous delivery wire into proximal anddistal segments; wherein a cross-sectional shape of at least a portionof the central stabilizer is different from a cross-sectional shape ofthe distal segment of the discontinuous delivery wire; and wherein atleast a portion of the proximal segment of the discontinuous deliverywire lies within the hollow proximal delivery wire.
 2. The device ofclaim 1, wherein each of the proximal and distal capture members furthercomprises an open end and a tapered end, a frame component coupled to aencasement sleeve, said encasement sleeve extending between said openend and said tapered end.
 3. The device of claim 2, wherein saidproximal frame component and distal frame component comprise aself-expanding material configured to have a collapsed configuration andan expanded configuration.
 4. The device of claim 2, wherein the centralcot stabilizer comprises a self-expanding material configured to have acollapsed configuration and an expanded configuration.
 5. The device ofclaim 2, wherein the central clot stabilizer is manually adjustable. 6.The device of claim 5, wherein an expansion state of the manuallyadjustable central clot stabilizer comprises a fully collapsed state, afully expanded state, or any expansion state therebetween.
 7. The deviceof claim 3, wherein the device further comprises a catheter.
 8. Thedevice of claim 7, wherein collapsed configurations of the proximalcapture member, distal capture member, and central stabilizer residewithin the catheter.
 9. The device of any of claims 1-8, wherein atleast one capture member further comprises a support arm.
 10. The deviceof claim 9, wherein the support arm is coupled to the respectivedelivery wire and the respective frame component.
 11. The device ofclaim 2, wherein at least one capture member further comprises afastening component slidably coupled to the respective delivery wire,allowing a coupling angle of the respective frame component to beadjusted.
 12. The device of claim 2, wherein the encasement sleeves aredevoid of any fenestrations.
 13. The device of claim 2, wherein theencasement sleeves comprise a woven material of at least one of thefollowing: a polymer, a metal, and any combination thereof.
 14. Thedevice of claim 2, wherein the encasement sleeves comprise a soft andflexible material.
 15. The device of claim 2, wherein the encasementsleeves comprise a self-expanding material configured to bias theencasement sleeve into an expanded configuration.
 16. The device ofclaim 2, wherein each encasement sleeve covers at least a portion of asurface of the frame component to which it is coupled.
 17. The device ofclaim 2, wherein at least one of the proximal frame component, thedistal frame component, or the central stabilizer is configured todeliver a therapeutic substance to said obstruction.
 18. The device ofclaim 1, further comprising a radiopaque marker.
 19. The device of claim1, wherein at least a portion of the proximal hollow delivery wirecomprises a furrowed semi-cylinder that allows at least a portion thecentral stabilizer to be withdrawn into the proximal encasement sleeve.20. The device of claim 19, wherein the furrowed semi-cylinder comprisesa length that is equal to or greater than a central stabilizer length toallow the entire length of the central stabilizer to reside within theproximal encasement sleeve.
 21. The device of claim 2, wherein aproximal frame component diameter is different from a distal framecomponent diameter.
 22. A device for remove an obstruction in a lumencomprising: a proximal capture member; a distal capture member; and acentral stabilizer wherein the proximal capture member comprises aproximal encasement sleeve and a hollow proximal delivery wire; whereinthe distal capture member comprises a distal encasement sleeve and adistal delivery wire; wherein the central stabilizer comprises a centraldelivery wire.
 23. The device of claim 22, wherein the each of theproximal and distal capture members further comprises an open end and atapered end, a frame component coupled to a encasement sleeve, saidencasement sleeve extending between said open end and said tapered end.24. The device of claim 23, wherein said proximal frame component anddistal frame component comprise a self-expanding material configured tohave a collapsed configuration and an expanded configuration.
 25. Thedevice of claim 23, wherein the central cot stabilizer comprises aself-expanding material configured to have a collapsed configuration andan expanded configuration.
 26. The device of claim 23, wherein thecentral clot stabilizer is manually adjustable.
 27. The device of claim25, wherein an expansion state of the manually adjustable central clotstabilizer comprises a fully collapsed state, a fully expanded state, orany expansion state therebetween.
 28. The device of claim 24, whereinthe device further comprises a catheter.
 29. The device of claim 28,wherein collapsed configurations of the proximal capture member, distalcapture member, and central stabilizer reside within the catheter. 30.The device of claim 29, wherein at least one capture member furthercomprises a support arm.
 31. The device of claim 30, wherein the supportarm is coupled to the respective delivery wire and the respective framecomponent.
 32. The device of claim 23, wherein at least one capturemember further comprises a fastening component slidably coupled to therespective delivery wire, allowing a coupling angle of the respectiveframe component to be adjusted.
 33. The device of claim 23, wherein theencasement sleeves are devoid of any fenestrations.
 34. The device ofclaim 23, wherein the encasement sleeves comprise a woven material of atleast one of the following: a polymer, a metal, and any combinationthereof.
 35. The device of claim 23, wherein the encasement sleevescomprise a soft and flexible material.
 36. The device of claim 23,wherein the encasement sleeves comprise a self-expanding materialconfigured to bias the encasement sleeve into an expanded configuration.37. The device of claim 2, wherein each encasement sleeve covers atleast a portion of a surface of the frame component to which it iscoupled.
 38. The device of claim 2, wherein at least one of the proximalframe component, the distal frame component, or the central stabilizeris configured to deliver a therapeutic substance to said obstruction.39. The device of claim 1, further comprising a radiopaque marker. 40.The device of claim 23, wherein a proximal frame component diameter isdifferent from a distal frame component diameter.
 41. The device ofclaim 22, wherein a cross-sectional shape of at least a portion of thecentral stabilizer is different from a cross-sectional shape of thecentral delivery wire.
 42. The device of claim 22, wherein the centraldelivery wire and the distal delivery wire lie adjacently within thehollow proximal delivery wire.
 43. The device of claim 22, wherein thecentral delivery wire and distal delivery wire are orientedconcentrically within the hollow proximal tube.
 44. The device of claim24, wherein at least a portion of the central delivery wire resideswithin at least a portion of the distal delivery wire.
 45. The device ofclaim 44, wherein at least a portion of the distal delivery wirecomprises a furrowed semi-cylinder that allows at least a portion thecentral stabilizer to be maneuvered into the distal encasement sleeve.46. The device of claim 45, wherein the furrowed semi-cylinder length isequal to or greater than the length of central stabilizer, enabling theentire length of the central stabilizer to be maneuvered into the distalencasement sleeve.